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BIOTOX BAC 2 (bacillus tetani, chlamydia trachomatis, streptococcus viridans, meningococcus nosode, phytolacca decandra, pneumococcinum, clostridium perfringens, dysentery bacillus, enterococcus faecalis, listeria monocytogenes, streptococcus agalactiae, streptococcus dysgalactiae, streptococcus mutans, streptococcus bovis, streptococcus uberis) liquid [The Wellness Center for Research and Education, Inc.]
Updated Date: Tue, 05 Oct 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 5, 2021 Category: Drugs & Pharmacology Source Type: alerts

PURELL EDUCATION HAND SANITIZER SF607 FOAM (benzalkonium chloride) liquid [GOJO Industries, Inc.]
Updated Date: Mon, 12 Jul 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - July 12, 2021 Category: Drugs & Pharmacology Source Type: alerts

BIOTOX T (bacillus tetani, ledum palustre) liquid [The Wellness Center For Research and Education]
Updated Date: Thu, 17 Jun 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - June 17, 2021 Category: Drugs & Pharmacology Source Type: alerts

Medline Industries Inc - Tissue Recovery Instrument Set - Class 2 Recall
Medline Tissue Recovery Instrument Set, Reorder #DYNJ64347A, packaged 3/case, Sterile, Rx. Convenience kit used to recover tissue, which can be used for medical research, education, or transplantation. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 10, 2021 Category: Medical Devices Source Type: alerts

Hershey Voluntarily Recalls Hershey ’s Chocolate Shell Topping Due to Undeclared Almonds
The Hershey Company (Hershey) today announced a voluntary recall of a single lot of Hershey ’s Chocolate Shell Topping in a 7.25-oz. (205g) bottle with UPC (346000) after learning that 1,700 bottles were incorrectly filled with Heath Shell Topping which is made with almonds. Hershey is initiating the (Source: FDA Food Safety)
Source: FDA Food Safety - May 5, 2021 Category: Food Science Authors: FDA Source Type: alerts

ENDOPURE TESTOS FOR WOMEN (hypothalamus suis, rna, sabal serrulata, dna, glandula suprarenalis suis, hydrocortisone (cortisol), hypophysis suis, testosterone, chelidonium majus, thuja occidentalis) liquid [The Wellness Center for Research and Education, Inc.]
Updated Date: Tue, 20 Apr 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - April 20, 2021 Category: Drugs & Pharmacology Source Type: alerts

BIOTOX PEST DETOX (glyphosate) liquid [The Wellness Center For Research and Education]
Updated Date: Thu, 18 Mar 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - March 18, 2021 Category: Drugs & Pharmacology Source Type: alerts

ALL FLU (aconitum napellus, arsenicum iodatum, bryonia (alba), eupatorium perfoliatum, gelsemium sempervirens, helix tosta, hydrogen, influenzinum, kreosotum, phosphorus, teucrium scorodonia, thuja occidentalis, veratrum viride, anas barbariae, hepatis et cordis extractum) pellet [The Wellness Center For Research and Education]
Updated Date: Wed, 10 Mar 2021 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - March 10, 2021 Category: Drugs & Pharmacology Source Type: alerts

HIGHER EDUCATION SPRING BREAK OIL-FREE BROAD-SPECTRUM SUNSCREEN SPF 30 lotion [Higher Education Skincare, LLC]
Updated Date: Wed, 13 Jan 2021 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - January 13, 2021 Category: Drugs & Pharmacology Source Type: alerts

HIGHER EDUCATION MAKE OUT READY MOISTURIZING LIP BALM SPF 15 lipstick [Higher Education Skincare, LLC]
Updated Date: Wed, 13 Jan 2021 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - January 13, 2021 Category: Drugs & Pharmacology Source Type: alerts

North American Rescue LLC. - 4 Inch Flat Responder Emergency Trauma Dressing - Class 2 Recall
4 In. Flat Responder Emergency Trauma Dressing part number 30-0171, packaged in kits labeled as follows: a) M-FAK Mini First Aid Kit; Kit Product Code: 80-0890 b) M-FAK Mini First Aid Kit, with Bleeding Control Dressing; Kit Product Code: 80-0891 c) M-FAK Mini First Aid Kit, Advance; Kit Product Code: 80-0892 d) M-FAK Mini First Aid Kit, Basic; Kit Product Code: 80-0913 e) M-FAK Mini First Aid Kit; Kit Product Code: 80-0914 f) Trauma and First Aid Kit; Kit Product Code: 80-0947 g) Trauma and First Aid Kit; Kit Product Code: 80-0948 h) Trauma and First Aid Kit; Kit Product Code: 80-1047 i) Trauma and First Aid Kit ...
Source: Medical Device Recalls - September 26, 2020 Category: Medical Devices Source Type: alerts

Goodie Girl Tribeca LLC Recalls Goodie Girl Magical Animal Crackers Due to Undeclared Wheat
Goodie Girl Tribeca LLC announced today it is voluntarily recalling 389 cases of a single date code of 7 oz. Goodie Girl Magical Animal Crackers, with a “best by” date of Jan 11, 21A3, after learning that the product may contain undeclared wheat ingredients. People who have an allergy or severe sens (Source: FDA Food Alergies)
Source: FDA Food Alergies - September 11, 2020 Category: Food Science Authors: FDA Source Type: alerts

B & G Foods Issues Voluntary Allergy Alert on Undeclared Milk in a Limited Number of Boxes of Back to Nature ® Organic Rosemary & Olive Oil Stoneground Wheat Crackers
B&G Foods announced today it is voluntarily recalling 1,502 cases of a single date code of 6 oz. Back to Nature Organic Rosemary& Olive Oil Stoneground Wheat Crackers, with a “best by” date of APR 07 2021, after learning that the product may contain undeclared milk ingredients. (Source: FDA Food Safety)
Source: FDA Food Safety - August 26, 2020 Category: Food Science Authors: FDA Source Type: alerts

Philips North America, LLC - Philips HeartStart MRx - Class 2 Recall
Philips HeartStart MRx, Monitor/Defibrillators with model numbers M3535A, M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9 - Product Usage: is intended for use in hospital and pre-hospital settings by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac life support or defibrillation. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 14, 2020 Category: Medical Devices Source Type: alerts

Hocoma AG - Lokomat Pro - Class 2 Recall
Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD ; 30004 LokomatPro L6.2 120V Kombi; 30005 LokomatPro L6.2 120V PE; 30683 LokomatPro L6.2 110V FD PE; 30684 LokomatPro L6.2 110V FD Kombi; 32001 LokomatPro L6.2 110V FD AD Product Usage: The intended use of the Lokomat is to support treadmill training to treat patients with walking disabilities caused by neurological, muscular or bone-related disorders. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 24, 2020 Category: Medical Devices Source Type: alerts